| Literature DB >> 26626770 |
Catherine G Chung1, Brian Poligone2.
Abstract
Mycosis fungoides (MF) and its leukemic variant, Sézary syndrome (SS), are malignancies of skin-homing T cells that comprise the majority of cutaneous T cell lymphomas (CTCL). Treatment of CTCL is limited and can be approached by skin-directed therapy or systemic therapy. Recent investigations into the pathogenesis of MF and SS have broadened the therapeutic targets; here, we review emerging concepts in the pathogenesis of MF and SS as well as novel and traditional systemic therapies for MF and SS. These include histone deacetylase inhibitors (vorinostat, romidepsin, panobinostat, and belinostat), monoclonal antibodies (alemtuzumab, brentuximab vedotin, and mogamulizumab) and single-agent cytotoxic chemotherapeutic agents (e.g., pralatrexate, doxorubicin, bendamustine, and forodesine), as well as multi-agent chemotherapy regimens.Entities:
Keywords: Chemotherapy; Cutaneous T cell lymphoma; Monoclonal antibodies; Pathogenesis
Mesh:
Substances:
Year: 2015 PMID: 26626770 DOI: 10.1007/s11899-015-0293-y
Source DB: PubMed Journal: Curr Hematol Malig Rep ISSN: 1558-8211 Impact factor: 3.952